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Merck
CN

206547

对碘苯甲酸

98%

别名:

4-碘苯甲酸, 对碘苯甲酸, 碘代苯-4-羧酸

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关于此项目

线性分子式:
IC6H4CO2H
化学文摘社编号:
分子量:
248.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-603-2
Beilstein/REAXYS Number:
1860232
MDL number:
Assay:
98%
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Quality Level

assay

98%

mp

270-273 °C (lit.)

functional group

carboxylic acid, iodo

SMILES string

OC(=O)c1ccc(I)cc1

InChI

1S/C7H5IO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)

InChI key

GHICCUXQJBDNRN-UHFFFAOYSA-N

Application

4-碘苯甲酸被用于原位合成[羟基(4-羧基苯基)碘]离子,这有助于裂解各种烯烃


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Prem P Thottumkara et al.
Organic letters, 12(24), 5640-5643 (2010-11-18)
A facile and operationally convenient catalytic procedure for oxidative cleavage of alkenes is described. In situ formed [hydroxy(4-carboxyphenyl)iodonium]ion, 2, from the oxidation of 4-iodobenzoic acid, 1, has been shown to facilitate the cleavage of a variety of alkenes in presence
Peggy E Williams et al.
Journal of the American Society for Mass Spectrometry, 29(9), 1848-1860 (2018-06-06)
In the gas phase, arylperoxyl forming reactions play a significant role in low-temperature combustion and atmospheric processing of volatile organic compounds. We have previously demonstrated the application of charge-tagged phenyl radicals to explore the outcomes of these reactions using ion
Toshiaki Taira et al.
Journal of oleo science, 67(9), 1107-1115 (2018-09-04)
In this study, an N-heterocyclic carbene (NHC)-based metallosurfactant (MS), NHC-PdMS, was synthesized, where Pd(II) was bound to the NHC framework via a robust Pd-carbene bond with NEt3 as a co-ligand. Surface tension measurements revealed that the critical micelle concentration (CMC)



全球贸易项目编号

货号GTIN
206547-5G04061838768711
206547-25G04061838768704